(Q41601398)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Mitochondrial DNA mutations in multiple symmetric lipomatosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

0 references

5

1 reference

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6 November 2019

author name string

T Klopstock

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

M Naumann

2

1 reference

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6 November 2019

P Seibel

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

B Shalke

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

H Reichmann

6

1 reference

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6 November 2019

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

Molecular and Cellular Biochemistry

6 November 2019

published in

1 reference

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6 November 2019

volume

174

1 reference

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6 November 2019

issue

1-2

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6 November 2019

page(s)

271-275

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309699%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1006877012241

6 November 2019

exact match

0 references

cites work

Familial multiple symmetric lipomatosis with peripheral neuropathy

1 reference

12 December 2020

Mitochondrial dysfunction in multiple symmetrical lipomatosis

1 reference

12 December 2020

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

1 reference

12 December 2020

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas

1 reference

12 December 2020

Clinical spectrum of mitochondrial DNA mutation at base pair 8344

1 reference

12 December 2020

Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple symmetric lipomatosis.

1 reference

12 December 2020

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation").

1 reference

12 December 2020

Failure to detect brown adipose tissue uncoupling protein mRNA in benign symmetric lipomatosis (Madelung's disease)

1 reference

12 December 2020

Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNA

1 reference

12 December 2020

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

12 December 2020

Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

1 reference

12 December 2020

Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration

1 reference

12 December 2020

Ekbom's syndrome: lipomas, ataxia, and neuropathy with MERRF

1 reference

12 December 2020

Neurological multisystem manifestation in multiple symmetric lipomatosis: a clinical and electrophysiological study

1 reference

12 December 2020

Neuropathy in multiple symmetric lipomatosis. Madelung's disease

1 reference

12 December 2020

Sensory, motor, and autonomic neuropathy in patients with multiple symmetric lipomatosis

1 reference

12 December 2020

Mitochondrial abnormalities are not invariably present in neurologic syndromes associated with multiple symmetric lipomatosis

1 reference

12 December 2020